Intraoperative ICG plasma disappearance rate helps to predict absence of early postoperative complications after orthotopic liver transplantation
Early postoperative complications after orthotopic liver transplantation (OLT) are a common problem in intensive care medicine. Adequate assessment of initial graft function remains difficult, however, plasma disaperance rate of indocyanine green (PDR ICG ) may have an additional diagnostic and prog...
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Published in | Journal of clinical monitoring and computing Vol. 27; no. 5; pp. 591 - 598 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.10.2013
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Early postoperative complications after orthotopic liver transplantation (OLT) are a common problem in intensive care medicine. Adequate assessment of initial graft function remains difficult, however, plasma disaperance rate of indocyanine green (PDR
ICG
) may have an additional diagnostic and prognostic value in this setting. We retrospectively evaluated the ability of
intraoperative
PDR
ICG
values to predict absence of early postoperative complications in 62 subjects. PDR
ICG
was measured non-invasively by pulse dye densitometry during surgery and was correlated with initial graft function. At the end of surgery, PDR
ICG
was higher in patients without complications: 24.9 % min
−1
(n = 40) versus 21.0 % min
−1
, (n = 22;
p
= 0.034). An area under the ROC curve (AUROC) for PDR
ICG
was 0.70, while the AUROC for pH, lactate and PT at ICU admission were 0.53, 0.50 and 0.46, respectively. The AUROC of serum bilirubin and PT at postoperative day 5 were 0.68 and 0.49, respectively. The optimal cut-off PDR
ICG
value for predicting absence of development early postoperative complications was determined to be 23.5 % min
−1
with 72.4 % sensitivity and 71.0 % specificity. Intraoperative point-of-care PDR
ICG
measurement during OLT already predicts absence of early postoperative complications, better and earlier than clinically used laboratory parameters. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1387-1307 1573-2614 |
DOI: | 10.1007/s10877-013-9474-1 |